[头孢他啶-阿维巴坦和头孢托ozane-他唑巴坦对临床分离的肠杆菌科和假单胞菌的体外活性:来自突尼斯创伤中心和烧伤病房的结果]。

Annals of burns and fire disasters Pub Date : 2025-03-31 eCollection Date: 2025-03-01
Z Megdiche, M Lamloumi, B Maamar, S Dhraief, A A Messadi, L Thabet
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引用次数: 0

摘要

抗生素耐药性是一个不断升级的公共卫生挑战,特别是在肠杆菌科和铜绿假单胞菌中。在突尼斯一家烧伤中心进行的这项研究中,我们从主要住院患者中收集了307株非冗余肠杆菌科菌株,其中大多数是烧伤重症监护病房(59%),主要鉴定的菌株是肺炎克雷伯菌(34.8%)。我们评估了头孢他啶-阿维巴坦(CZA)和头孢洛赞-他唑巴坦(CT)两种抗生素的疗效。结果显示,CZA总耐药率为11.7%,CT总耐药率为25.7%。CZA被证明是所有测试抗生素中第二敏感的分子,仅次于磷霉素。第三代头孢菌素耐药菌株中,对CZA敏感的占73.3%,对CT敏感的占41.5%。79株ct耐药菌株中,8株为ESBL产生菌,22株为高水平头孢菌素酶,33株携带blaNDM, 12株携带blaOXA48, 4株同时携带blaNDM和blaOXA-48。事实上,blaNDM是最普遍的碳青霉烯酶。铜绿假单胞菌(n=161)对CZA和CT的耐药率分别为42.2%和47.8%。这些抗生素是仅次于氨曲南的第二和第三活跃的β -内酰胺类抗生素。在71株CZA和耐碳青霉烯P. aeruginosa菌株中,产生VIM2的菌株占54.1%。在我们的研究中,肠杆菌科对CZA和CT的耐药性相对较高。然而,CZA仍然是碳青霉烯耐药生物引起的感染的一种补救性治疗,只有在有文献记载并且在β-内酰胺类药物中没有其他替代品的情况下,才应该考虑使用CZA。对于P. aeruginosa, CZA目前代表了对CAZ-R菌株最活跃的β-内酰胺和第二活跃的分子,包括产生碳青霉烯酶的分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[In vitro activity of ceftazidime- avibactam and ceftolozane- tazobactam against clinical isolates of enterobacteriaceae and pseudomonas æruginosa: results from a trauma center and burn unit in tunisia].

Antibiotic resistance is an escalating public health challenge, particularly among Enterobacteriaceae and Pseudomonas aeruginosa. In this study conducted at a burn center in Tunisia, we collected 307 non-redundant strains of Enterobacteriaceae from predominantly hospitalized patients, with a majority in the burn intensive care unit (59%), the primary identified species being Klebsiella pneumoniae (34.8%). We evaluated the efficacy of two antibiotics, ceftazidime-avibactam (CZA) and ceftolozane-tazobactam (CT). The results revealed that the overall resistance to CZA was 11.7%, while to CT it was 25.7%. CZA proved to be the second most sensitive molecule among all tested antibiotics, following fosfomycin. Among strains resistant to third-generation cephalosporins, 73.3% were sensitive to CZA, and 41.5% to CT. Out of seventy-nine CT-resistant strains, eight were ESBL producers, twenty-two were high-level cephalosporinases, thirty-three carried blaNDM, twelve carried blaOXA48, and four carried both blaNDM and blaOXA-48. Indeed, blaNDM were the most prevalent carbapenemases. For Pseudomonas aeruginosa strains (n=161), resistance to CZA was 42.2%, and to CT it was 47.8%. These antibiotics ranked as the second and third most active beta-lactams after aztreonam. Among the 71 strains of CZA and carbapenem-resistant P. aeruginosa, 54.1% produced VIM2. Resistance to enterobacteriaceae against CZA and CT is relatively high in our study. However, CZA remains a salvage therapy for infections caused by carbapenem-resistant organisms, and its use should be considered only after documentation and in the absence of other alternatives among β-lactams. For P. aeruginosa, CZA currently represents the most active β-lactam against CAZ-R strains and the second most active molecule overall, including those producing carbapenemases.

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